A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492708



Internal ID21150261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99303764..99304186hg38UCSC Ensembl
chr13:99956018..99956440hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38423
hg19423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016408
Samples
Known GenesGPR183, MIR548AN, UBAC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492708
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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